
Faculty, Staff and Student Publications
Publication Date
1-1-2022
Journal
Frontiers in Immunology
Abstract
The advent of cellular immunotherapy in the clinic has entirely redrawn the treatment landscape for a growing number of human cancers. Genetically reprogrammed immune cells, including chimeric antigen receptor (CAR)-modified immune effector cells as well as T cell receptor (TCR) therapy, have demonstrated remarkable responses across different hard-to-treat patient populations. While these novel treatment options have had tremendous success in providing long-term remissions for a considerable fraction of treated patients, a number of challenges remain. Limited
Keywords
cell engineering, gene editing, immune effector cell, cell therapy, CAR (chimeric antigen receptor), CRISPR screening
DOI
10.3389/fimmu.2022.1063303
PMID
36483551
PMCID
PMC9723254
PubMedCentral® Posted Date
November 2022
PubMedCentral® Full Text Version
Post-print
Published Open-Access
yes
Included in
Bioinformatics Commons, Biomedical Informatics Commons, Medical Sciences Commons, Oncology Commons
Comments
PMID: 36483551